- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05097066
Patterns and Outcomes of Neurosurgery in England Over a Five-year Period
Patterns and Outcomes of Neurosurgery in England Over a Five-year Period: a National Retrospective Cohort Study
Neurosurgical practice has seen many important changes over several decades with advances in treatments and the types of patients treated. Neurosurgical procedures have evolved, and as outcomes have improved the number of patients being treated has increased.
There are no recent evaluations of national neurosurgical practice in the United Kingdom (UK), with the last prospective cohort studies being Safe Neurosurgery 1993 and Safe Neurosurgery 2000. More recent studies of neurosurgical services have been based on data from single institutions or surgeons and these may not give a representative picture of practice nationally.
Recent national quality improvement programmes for neurosurgery in England (such as the National Neurosurgical Audit Programme (NNAP) and Cranial Neurosurgery and Spinal Surgery Getting It Right First Time (GIRFT) Programmes) have focused on using national hospital administrative datasets. To be effective, quality improvement initiatives require robust outcome measures and quality (process) indicators. Currently, there is a lack of validated quality indicators for neurosurgery, with practice often being described using generic measures such as readmission and reoperation rates and length of stay. Many studies have been able to derive these common outcome measures, but it may also be possible to produce indicators specific to neurosurgery.
The aim of this observational study was firstly to describe the current pattern of neurosurgical admissions and procedures in England, and thereby given an overview of the epidemiology of neurosurgical patients. Secondly, it aims to investigate the range of outcome measures that might be produced from hospital administrative data and use these to assess the quality of care in neurosurgery.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All admissions to neurosurgical units in the National Health Service (NHS) in England.
Exclusion Criteria:
- Records with poor quality data (e.g. no data for clinical diagnoses).
- Patients under 18 years that were admitted to an adult neurosurgical unit.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Elective neurosurgery
Any elective neurosurgical procedure.
|
Any neurosurgical procedure in the National Neurosurgical Audit Programme (NNAP) Coding Framework of neurosurgical procedures.
|
|
Non-elective neurosurgery
Any non-elective neurosurgical procedure.
|
Any neurosurgical procedure in the National Neurosurgical Audit Programme (NNAP) Coding Framework of neurosurgical procedures.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Length of stay
Time Frame: From date of admission to date of discharge from hospital; assessed up to 60 months.
|
Length of the hospital admission to neurosurgery
|
From date of admission to date of discharge from hospital; assessed up to 60 months.
|
|
Additional inpatient neurosurgical procedure rate
Time Frame: From date of admission to date of discharge from hospital; assessed up to 60 months.
|
A further neurosurgical procedure in admissions where patients have had a primary (main) neurosurgical procedure.
|
From date of admission to date of discharge from hospital; assessed up to 60 months.
|
|
Proportion of patients discharged home
Time Frame: Determined on date of discharge from hospital; assessed up to 60 months.
|
Proportion of patients discharged to their normal address.
|
Determined on date of discharge from hospital; assessed up to 60 months.
|
|
In-patient mortality rate
Time Frame: From date of the neurosurgical procedure through date of death from any cause (in-patient deaths only); assessed up to 60 months.
|
In-patient mortality after a neurosurgical procedure.
|
From date of the neurosurgical procedure through date of death from any cause (in-patient deaths only); assessed up to 60 months.
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Ryan Mathew, University of Leeds
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NNAP002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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